For my part the way I understand my gender is absolutely influenced by my autism, but the way I experience it is perhaps not? Gender things feel right or they don’t feel right, those aspects that I claim and embrace seem inherently autigender (to me), but the senses that originate that stuff aren’t processed, they are experienced.

tbh even with helpful explanations I’m finding the concepts involved very nebulous and hard to grasp, but that’s okay.

Also now that I think about it, whenever I needed a new watch I would usually try to get the same model, and I got really upset when that wasn't an option. I was super passionate about watches and time back then, but I think it was only because it helped make sense of school's constant transitions.

These days, or even back then at home, I'd prefer to forget about time and just go at my own pace.

Thinking back to my earliest school memories, I constantly felt like I was being buffeted around and I was always asking about time to know when story time or nap time or lesson time or lunch time or play time or whenever was starting or ending.

School is constant mode-switching, I wonder if I'd have done better if each school day was just one thing?

I remember liking sports days even though I didn't particularly like sports. It makes sense now though: one mode for the whole day, more comfortable clothes, and sitting in the grass looking at the trees around school were so chilling.

I never liked the noise though, and always resented any event I had to participate in.

One of the chapters is sort of highlighting how the way we mask indicates who we are under the mask, and gives pointers to remembering the events that made us hide those parts of ourselves.

I had a moment where I was like…. “Omfg, for a moment in my life, I was super bright! I was so loud and energetic!”

And then a few minutes later, my most childlike and cheery headmate chimed in like “Yep, I did tell you!”

Changing the CW so I can talk about not-autism things in this thread like tics, such as:

I sometimes have tics that feel like I’m trying to express something but get frustrated that I’m not being understood. All I’m doing is just saying “banana” over and over, and getting frustrated I haven’t expressed it in a particular way. What way? I have no idea! This happens even when I’m alone.

Had a huge piece of tooth come loose today and getting it out was not fun (I almost fainted lol).

Anyway I realised the reason I haven't seen a dentist since I was a child is largely because of autism. To find an NHS dentist you need to be constantly calling practices and asking until they have a slot, impossible for me. But now I know I'm autistic, instead of being ashamed and just living with it, I can ask my mum for help!

In theory I could have just done that all along, but the feeling of "I'm supposed to be able to do this!" is so powerful, but accepting there are just some things you can't do and that's okay? Revolutionary.

There's a fair bit about this in Unmasking Autism actually, in a less individualistic society I'd never have even noticed this was such a struggle. I'd just have asked for help without years of stress and worry.

Just got a call about my psychological assessment, it took almost a year to get the appointment and then it was reviewed in a little over a week.

The result is, yep, I have tics and they are probably related to my autism somehow. The recommendation is mostly that I ought to reach out to autistic orgs and talk to them about it.

Which, I guess is good? It’s probably not something more serious that I need to worry about.

But also, I think I’m pretty upset about it? Mostly because part of me was hoping there would just be something causing the tics that could be outright fixed.

I have found since I figured out I’m autistic and embraced stim regulation I’ve ticced less in private… but… tbh I hate that I tic. Hate it. And now I just have to face that I’ll have to live with it.

And I’ll probably never know why my tics became so much more prominent over just a few months, I have theories but now I know that certainty is not an option.

I guess I should have seen this coming tbh, I’ve done a lot of research myself and didn’t find any concrete answers, but I’d still hoped someone else could give me that.

Another one I saw in a compilation that made me go !!!!!!!

Discovering sensory sensitivities later in life can absolutely feel like an infohazzard! I am leaning towards thinking it is better to know and I get to feel more real and be able to solve some of the problems I now recognise, but also it can be super overpowering still
https://vm.tiktok.com/ZGJxaP4xN/

Also ngl it makes me super wary of things I *need* to do.

Case in point: I've needed to shower for maybe a week now? I'd been avoiding it because it is just so overwhelming. This morning I finally thought "fuck it, I'm in a good mood and feeling capable! Let's do it!"

And then I proceeded to have an AWFUL 30 seconds where I felt every wet and hot drop of water slamming into me and running through my hair, I might have screeched, I don't know.

I just realised, if my tics and autism are connected,

that means I have autis tics!

Looking up the local autism group that the psychologist recommended, and see they associate with the police *a lot*…

Yeah I’m going to be honest I’d rather check out the other one with puzzle pieces all over their website that seems like it’s 99% for autism mums.

I can definitely imagine an argument (however iffy) in favour of a group working with police for the purposes of training and mitigating police mistreatment on the basis of them just not knowing about autism but…

You’re retweeting the police commissioner on shit that has nothing to do with autism, using the group account too. And somehow you are also getting funding from the police?

That doesn’t seem safe at all to me. Big pass.

The psychologist did also recommend a few not-autism-related things, but they are all either CBT (been there) and/or trauma recovery/support (which I think I’m mostly done with by now).

It’s weird that realising I’m autistic is a lot of learning that things were just not made for me, and then I find out that even the things that were made for me aren’t really for me.

Anyway I don’t think I really *need* anything besides information right now, and I’m not having any difficulty getting that. I think most of this psych process is just so they can feel they aren’t completely abandoning me once I’m discharged.

All I needed from them was to know if my tics could be helped or explained and I got the answer, next I can figure out how I deal with that answer on my own.

Me (learning about how some people with sensory issues can find lights/sounds or other stimulation to be very painful): Wow that’s rough, I’m glad that doesn’t happen to me.

Me (hearing a sharp sound in a bright room): Ah! Ow!

Ugh even the little tinkle sound ivory made when sending that toot, I felt it in my neck.

Anyway I’m having a particularly sensitive afternoon I guess, but I’m just trying to enjoy how funny it is that I continue to be completely oblivious about what my own experience is, even when I’m trying to focus on it. Of course I’ve dealt with painful light, sounds, textures, smells, etc… but only now do I realise OH, that pain is pain! It counts as pain!

Great, turning my volume all the way down it still makes the noise, gonna put my iPad under a pillow to send this one but I had a thought I want to share:

It’s interesting how something as apparent as pain can be there and not noticed because like, it wasn’t supposed to be there. And I don’t mean in the sense that I shouldn’t be experiencing pain, but that this pain in particular was not socially recognised so I was unable to truly see it for what it was.

Unlocked another memory of doing autistic shit as a child:

When I was really young, I loved to answer the front door. LOVED IT. I’ve had a much more troubled history with that since then, but at the time it was kind of predictable, it was only ever one of three things and I could excel at the appropriate responses to each:
- Post, I take the post upstairs to my parents
- Guests, I go up and tell my parents
- My bossy friend, I do pretty much whatever he wants to do

BUT!

One afternoon I heard the doorbell, rushed excitedly to the door, swung it open…

And there stood a random kid from school I didn’t talk to, who smiled and said “trick or treat!”

I immediately slammed the door shut, locked it, and ran upstairs. I was not prepared for Halloween lol, and so yeah I didn’t excitedly rush to the front door after that.

See, every year at about this time I’ll post something like “we’re not destroying the environment fast enough lol” because I’m having a hard time with hay fever

Now, I realise “there’s probably a link between sensory processing issues and hay fever symptoms!” Since I understand this possibility I can look for help specific to autistics dealing with hay fever

But it’s so much harder to do because all the results are not that, they are from people outside of autism looking in

Anyway in the end the best thing I could do was just research hay fever in general and note how my experience differed.

Turns out, hay fever isn’t usually painful or overwhelming. For most people it’s just a bunch of extra discomfort while your face does gross things. For me it’s like I have millions of minuscule needle monsters scratching the inside of my face, it dominates my entire experience and after it goes on for a while it HURTS.

None of this is helped by parents noting that their kids have more meltdowns during allergy season, or that there appears to be a link between occurrence of autism and allergies. But those seem to be all the results when I look for hay fever and autism info together.

I just wanted to know I wasn’t alone, and those are not sources I can trust. I’d rather have found something like this thread - a personal account to say “yeah this happens”